Sigglekow Finn, Horsburgh Simon, Parkin Lianne
Department of Preventive and Social Medicine, Otago Medical School-Dunedin Campus, University of Otago, Dunedin, New Zealand.
Pharmacoepidemiology Research Network, University of Otago, Dunedin, New Zealand.
PLoS One. 2020 Nov 19;15(11):e0242424. doi: 10.1371/journal.pone.0242424. eCollection 2020.
Maintaining adherence to statins reduces the risk of an initial cardiovascular disease (CVD) event in high-risk individuals (primary prevention) and additional CVD events following the first event (secondary prevention). The effectiveness of statin therapy is limited by the level of adherence maintained by the patient. We undertook a nationwide study to compare adherence and discontinuation in primary and secondary prevention patients.
Dispensing data from New Zealand community pharmacies were used to identify patients who received their first statin dispensing between 2006 and 2011. The Medication Possession Ratio (MPR) and proportion who discontinued statin medication was calculated for the year following first statin dispensing for patients with a minimum of two dispensings. Adherence was defined as an MPR ≥ 0.8. Previous CVD was identified using hospital discharge records. Multivariable logistic regression was used to control for demographic and statin characteristics.
Between 2006 and 2011 289,666 new statin users were identified with 238,855 (82.5%) receiving the statin for primary prevention compared to 50,811 (17.5%) who received it for secondary prevention. The secondary prevention group was 1.55 (95% CI 1.51-1.59) times as likely to be adherent and 0.67 (95% CI 0.65-0.69) times as likely to discontinue statin treatment than the primary prevention group. An early gap in statin coverage increased the odds of discontinuing statin treatment.
Adherence to statin medication is higher in secondary prevention than primary prevention. Within each group, a range of demographic and treatment factors further influences adherence.
坚持服用他汀类药物可降低高危个体首次发生心血管疾病(CVD)事件的风险(一级预防),以及首次事件后额外CVD事件的风险(二级预防)。他汀类药物治疗的有效性受到患者坚持程度的限制。我们进行了一项全国性研究,以比较一级和二级预防患者的坚持程度和停药情况。
利用新西兰社区药房的配药数据,确定在2006年至2011年间首次接受他汀类药物配药的患者。计算至少有两次配药的患者在首次配药后一年的药物持有率(MPR)和停用他汀类药物的比例。坚持程度定义为MPR≥0.8。使用医院出院记录确定既往CVD情况。采用多变量逻辑回归来控制人口统计学和他汀类药物特征。
在2006年至2011年间,共确定了289,666名新的他汀类药物使用者,其中238,855名(82.5%)接受他汀类药物进行一级预防,50,811名(17.5%)接受二级预防。与一级预防组相比,二级预防组坚持用药的可能性是其1.55倍(95%CI 1.51 - 1.59),停用他汀类药物治疗的可能性是其0.67倍(95%CI 0.65 - 0.69)。他汀类药物覆盖的早期差距增加了停用他汀类药物治疗的几率。
二级预防中他汀类药物的坚持程度高于一级预防。在每组中,一系列人口统计学和治疗因素进一步影响坚持程度。